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Identification and expression profile analysis of the SnRK2 gene family in cucumber

The sucrose non-fermenting-1-related protein kinase 2 (SnRK2) is a plant-specific type of serine/threonine protein kinase that plays an important role in the physiological regulation of stress. The objective of this study was to identify and analyze the members of the SnRK2 gene family in cucumber a...

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Autores principales: Wan, Zilong, Luo, Shilei, Zhang, Zeyu, Liu, Zeci, Qiao, Yali, Gao, Xueqin, Yu, Jihua, Zhang, Guobin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508882/
https://www.ncbi.nlm.nih.gov/pubmed/36164601
http://dx.doi.org/10.7717/peerj.13994
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author Wan, Zilong
Luo, Shilei
Zhang, Zeyu
Liu, Zeci
Qiao, Yali
Gao, Xueqin
Yu, Jihua
Zhang, Guobin
author_facet Wan, Zilong
Luo, Shilei
Zhang, Zeyu
Liu, Zeci
Qiao, Yali
Gao, Xueqin
Yu, Jihua
Zhang, Guobin
author_sort Wan, Zilong
collection PubMed
description The sucrose non-fermenting-1-related protein kinase 2 (SnRK2) is a plant-specific type of serine/threonine protein kinase that plays an important role in the physiological regulation of stress. The objective of this study was to identify and analyze the members of the SnRK2 gene family in cucumber and lay a foundation for further exploration of the mechanism of CsSnRK2 resistance to stress. Here, 12 SnRK2 genes were isolated from cucumber and distributed on five chromosomes, phylogenetic clustering divided these into three well-supported clades. In addition, collinearity analysis showed that the CsSnRK2 gene family underwent purifying selection pressure during evolution. CsSnRK2 genes of the same group have similar exons and conserved motifs, and intron length may be a specific imprint for the evolutionary amplification of the CsSnRK2 gene family. By predicting cis elements in the promoter, we found that the promoter region of CsSnRK2 gene members had various cis-regulatory elements in response to hormones and stress. Relative expression analysis showed that CsSnRK2.11 (group II) and CsSnRK2.12 (group III) were strongly induced by ABA, NaCl and PEG stress; whereas CsSnRK2.2 (group III) was not activated by any treatment. The response of group I CsSnRK2 to ABA, NaCl and PEG was weak. Furthermore, protein interaction prediction showed that multiple CsSnRK2 proteins interacted with four proteins including protein phosphatase 2C (PP2C), and it is speculated that the CsSnRK2 genes may also an independent role as a third messenger in the ABA signaling pathway. This study provides a reference for analyzing the potential function of CsSnRK2 genes in the future research.
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spelling pubmed-95088822022-09-25 Identification and expression profile analysis of the SnRK2 gene family in cucumber Wan, Zilong Luo, Shilei Zhang, Zeyu Liu, Zeci Qiao, Yali Gao, Xueqin Yu, Jihua Zhang, Guobin PeerJ Agricultural Science The sucrose non-fermenting-1-related protein kinase 2 (SnRK2) is a plant-specific type of serine/threonine protein kinase that plays an important role in the physiological regulation of stress. The objective of this study was to identify and analyze the members of the SnRK2 gene family in cucumber and lay a foundation for further exploration of the mechanism of CsSnRK2 resistance to stress. Here, 12 SnRK2 genes were isolated from cucumber and distributed on five chromosomes, phylogenetic clustering divided these into three well-supported clades. In addition, collinearity analysis showed that the CsSnRK2 gene family underwent purifying selection pressure during evolution. CsSnRK2 genes of the same group have similar exons and conserved motifs, and intron length may be a specific imprint for the evolutionary amplification of the CsSnRK2 gene family. By predicting cis elements in the promoter, we found that the promoter region of CsSnRK2 gene members had various cis-regulatory elements in response to hormones and stress. Relative expression analysis showed that CsSnRK2.11 (group II) and CsSnRK2.12 (group III) were strongly induced by ABA, NaCl and PEG stress; whereas CsSnRK2.2 (group III) was not activated by any treatment. The response of group I CsSnRK2 to ABA, NaCl and PEG was weak. Furthermore, protein interaction prediction showed that multiple CsSnRK2 proteins interacted with four proteins including protein phosphatase 2C (PP2C), and it is speculated that the CsSnRK2 genes may also an independent role as a third messenger in the ABA signaling pathway. This study provides a reference for analyzing the potential function of CsSnRK2 genes in the future research. PeerJ Inc. 2022-09-21 /pmc/articles/PMC9508882/ /pubmed/36164601 http://dx.doi.org/10.7717/peerj.13994 Text en ©2022 Wan et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Agricultural Science
Wan, Zilong
Luo, Shilei
Zhang, Zeyu
Liu, Zeci
Qiao, Yali
Gao, Xueqin
Yu, Jihua
Zhang, Guobin
Identification and expression profile analysis of the SnRK2 gene family in cucumber
title Identification and expression profile analysis of the SnRK2 gene family in cucumber
title_full Identification and expression profile analysis of the SnRK2 gene family in cucumber
title_fullStr Identification and expression profile analysis of the SnRK2 gene family in cucumber
title_full_unstemmed Identification and expression profile analysis of the SnRK2 gene family in cucumber
title_short Identification and expression profile analysis of the SnRK2 gene family in cucumber
title_sort identification and expression profile analysis of the snrk2 gene family in cucumber
topic Agricultural Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508882/
https://www.ncbi.nlm.nih.gov/pubmed/36164601
http://dx.doi.org/10.7717/peerj.13994
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